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Jijun Wan

Showing results (11-20 of 21) with videos related to

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Nature Cardiovascular Research|October 25, 2024
Bone-marrow macrophage-derived GPNMB protein binds to orphan receptor GPR39 and plays a critical role in cardiac repairSivakumar Ramadoss, Juan Qin, Bo Tao, et al.
Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.
Cell Reports. Medicine|October 25, 2024
A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarctionShen Li, Bo Tao, Jijun Wan, et al.
Cell Stem Cell|June 16, 2026
ENPP1 blockade with a humanized monoclonal antibody enhances renal repair after acute kidney injuryLianjiu Su, Qihao Sun, Ziheng Zhou, et al.
Science Advances|January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signalingPaul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2024
Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephalyYue Huang, Kristy L Jay, Alden Yen-Wen Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 15, 2019
Diagnostic utility of transcriptome sequencing for rare Mendelian diseasesHane Lee, Alden Y Huang, Lee-Kai Wang, et al.
Science (New York, N.Y.)|April 24, 2004
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisJoanna C Jen, Wai-Man Chan, Thomas M Bosley, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Nature Cardiovascular Research|October 25, 2024
Bone-marrow macrophage-derived GPNMB protein binds to orphan receptor GPR39 and plays a critical role in cardiac repairSivakumar Ramadoss, Juan Qin, Bo Tao, et al.
Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.
Cell Reports. Medicine|October 25, 2024
A humanized monoclonal antibody targeting an ectonucleotidase rescues cardiac metabolism and heart function after myocardial infarctionShen Li, Bo Tao, Jijun Wan, et al.
Cell Stem Cell|June 16, 2026
ENPP1 blockade with a humanized monoclonal antibody enhances renal repair after acute kidney injuryLianjiu Su, Qihao Sun, Ziheng Zhou, et al.
Science Advances|January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signalingPaul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2024
Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephalyYue Huang, Kristy L Jay, Alden Yen-Wen Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 15, 2019
Diagnostic utility of transcriptome sequencing for rare Mendelian diseasesHane Lee, Alden Y Huang, Lee-Kai Wang, et al.
Science (New York, N.Y.)|April 24, 2004
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisJoanna C Jen, Wai-Man Chan, Thomas M Bosley, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Pageof 3